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Showing 1 – 9 of 9 results.
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21st Century Americanism: Nationally Representative Survey of the United States Population, 2004 (ICPSR 27601)

Released/updated on: 2015-04-02
Geographic coverage: United States
Time period: 2004-07-12--2004-10-08
The 21st Century Americanism survey was conducted to study (1) the multidimensional nature of American identity ("Americanism"); (2) resentment among Whites toward immigrants, Latinos, and Asians, fueled by perceptions that these groups violate the cherished norms that constitute American identity ("symbolic nativism"); (3) how perceptions of discrimination affect the process of "becoming American" among ethnic minorities ("reactive ethnicity"); and (4) the relationships among these issues and public opinion on policies that address ethnic change. The data collection began in July 2004 and was completed by October 2004. This nationally representative random-digit dial telephone survey has 2,800 respondents and includes oversamples of Blacks, Latinos, and Asians in the United States. It contains questions that allow for the examination of the causes and consequences of two facets of American identity: (1) how people define the normative content of American identity ("identity content"); and (2) the extent to which people think of themselves primarily as American rather than primarily as a member of a pan-ethnic (i.e., Latino or Asian) or national origin group ("identity attachment"). The survey can be used to test hypotheses regarding whether the alleged traditional consensus on what it means to be American is breaking down, or whether people are increasingly rejecting an American identity and instead prioritizing pan-ethnic or national origin identities. It can also be used to examine how these aspects of one's identity affect political attitudes and behaviors, such as trust in government, voting, and one's sense of obligation to the national community. Demographic variables include gender, age, country of origin, United States citizenship status, race, Hispanic origin, and language and educational attainment. Variables focusing on economic characteristics include employment status and household income.
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Asian Women Working in Massage Parlors in New York City and Los Angeles County, 2014-2016 (ICPSR 39387)

Released/updated on: 2025-07-28
Geographic coverage: New York City, United States, Los Angeles, California, New York (state)
Time period: 2014-01-01--2016-01-01

Media coverage has highlighted raids, mass arrests, and undercover stings of illicit massage parlors in United States cities and suburbs. This study defines "illicit," as a sub-set of massage parlors that purport to operate as legal businesses but where sexual services are illegally bought and sold. Although some media accounts have highlighted linkages between illicit massage parlors, human trafficking, and the fact that many of the workers are Asian immigrant women, the daily experiences of workers in illicit massage parlors are rarely reported from their own perspectives. To fill this gap in knowledge, researchers interviewed 116 Chinese and Korean women who reported that they had provided sexual services in a massage parlor setting in New York City or Los Angeles County. This data collection includes anonymized responses from these women about their demographic background, path to working in massage parlors, working conditions, social networks, sexual health and access to healthcare, victimization by clients and managers, and trust in law enforcement.

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Collaborative Psychiatric Epidemiology Surveys (CPES), 2001-2003 [United States] (ICPSR 20240)

Released/updated on: 2024-02-28
Geographic coverage: United States
Time period: 2001-01-01--2003-01-01
The Collaborative Psychiatric Epidemiology Surveys (CPES) were initiated in recognition of the need for contemporary, comprehensive epidemiological data regarding the distributions, correlates and risk factors of mental disorders among the general population with special emphasis on minority groups. The primary objective of the CPES was to collect data about the prevalence of mental disorders, impairments associated with these disorders, and their treatment patterns from representative samples of majority and minority adult populations in the United States. Secondary goals were to obtain information about language use and ethnic disparities, support systems, discrimination and assimilation, in order to examine whether and how closely various mental health disorders are linked to social and cultural issues. To this end, CPES joins together three nationally representative surveys: the NATIONAL COMORBIDITY SURVEY REPLICATION (NCS-R), the NATIONAL SURVEY OF AMERICAN LIFE (NSAL), and the NATIONAL LATINO AND ASIAN AMERICAN STUDY (NLAAS). These surveys collectively provide the first national data with sufficient power to investigate cultural and ethnic influences on mental disorders. In this manner, CPES permits analysts to approach analysis of the combined dataset as though it were a single, nationally representative survey. Each of the CPES surveys has been documented in a comprehensive and flexible manner that promotes cross-survey linking of key data and scientific constructs.
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Daily Experience in Adolescence and Biomarkers of Early Risk for Adult Health (ICPSR 35952)

Released/updated on: 2015-06-05
Geographic coverage: United States
This project conducts a 3-wave longitudinal study of adolescents and their caregivers from Mexican, Chinese, and European backgrounds in order to assess the impact of daily experience on biological indicators of early risk for adult health. It includes intensive behavioral assessments and detailed biological markers of health risk from both adolescents and their parents. Approximately 540 pairs of adolescents and their primary caregivers (180 from each ethnic group) are assessed when the adolescents are approximately 15-16, 17-18, and 19-20 years old. Each year, both adolescents and caregivers participate in interviews that include measures of global social factors and potential protective factors. Participants report daily experiences using a nightly diary checklist for 9 consecutive days. Salivary cortisol is obtained at 4 time points each day for 4 of these days in order to analyze HPA activity, and participants wear wrist actigraphs for the same 4 days to measure objective sleep behaviors. Blood pressure, BMI, and waist/hip ratio are assessed, and dried blood spots are obtained for the assessment of c-reactive-protein (CRP), cholesterol, and high density lipoproteins (HDL). Finally, peripheral blood samples are provided by a subsample of 120 families for the assessment of plasma interleukin-6 (IL-6), a pro-inflammatory cytokine, and for gene expression analyses of molecular signaling pathways driving inflammatory biology.
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Japanese-American Research Project (JARP): a Three-Generation Study, 1890-1966 (ICPSR 8450)

Released/updated on: 2006-01-12
Geographic coverage: United States
Time period: 1890-01-01--1966-01-01
This data collection is a sociohistorical study of the ways in which three generations (Issei, Nisei, and Sansei) of Japanese American families adapted to social, cultural, educational, occupational, and other institutions of American life. The study examines the experience of the first immigrants to the United States (Issei), and their children (Nisei) and grandchildren (Sansei). Interviews with Issei families stressed the difficulties faced by the immigrants during their early years in the United States, as well as aspects of social and cultural life. Interviews with Nisei included questions on employment, attitudes toward work, income, education, marriage, social relationships, discrimination, and religion. Topics covered in Sansei interviews included birth order, age, marital status, children, social relationships, occupation, industry, income, education, Japanese value systems, marital choices, influence of parents and grandparents, discrimination, religion, political attitudes, and migration.
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Study of Women's Health Across the Nation (SWAN), 1998-2001: Family Medical History From Visits 02, 03, and 04 (ICPSR 30181)

Released/updated on: 2014-02-13
Geographic coverage: Inkster, Hackensack, United States, Chicago, Ypsilanti, California, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 1998-02-15--2001-06-01
The Study of Women's Health Across the Nation (SWAN) is a multisite longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers, and women learn how mid-life experiences affect health and quality of life during aging. The study is co-sponsored by the National Institute on Aging (NIA) and the National Institute of Health (NIH), Office of Research on Women's Health. The study began in 1994. Between 1998 and 2001, 2,829 of the 3,302 women that joined SWAN participated in a collection of family history data. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Almeda and Contra Costa County, CA (University of California, Davis and Kaiser Permanente); Los Angeles, CA (University of California, Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures.
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Study of Women's Health Across the Nation (SWAN), 2003-2005: Visit 07 Dataset (ICPSR 31901)

Released/updated on: 2025-07-10
Geographic coverage: Inkster, Contra Costa County, Alameda County, United States, Chicago, Ypsilanti, California, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Boston, Pittsburgh
Time period: 2003-05-15--2005-01-31
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. Data were collected about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause. The study began in 1994. Between 2003 and 2005, 2,327 of the 3,302 women that joined SWAN were seen for their seventh follow-up visit. The research centers are located in the following communities: Ypsilanti and Inkster, MI (University of Michigan); Boston, MA (Massachusetts General Hospital); Chicago, IL (Rush Presbyterian-St. Luke's Medical Center); Alameda and Contra Costa County, CA (University of California-Davis and Kaiser Permanente); Los Angeles, CA (University of California-Los Angeles); Hackensack, NJ (Hackensack University Medical Center); and Pittsburgh, PA (University of Pittsburgh). SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. Though the New Jersey site was still part of the study, data was not collected from this site for the seventh visit. Demographic and background information includes age, language of interview, marital status, household composition, and employment.
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Study of Women's Health Across the Nation (SWAN): Visit 01 Dataset, [United States], 1997-1999 (ICPSR 29221)

Released/updated on: 2019-05-02
Geographic coverage: Detroit, United States, Chicago, California, Oakland, New Jersey, Michigan, Pennsylvania, Illinois, Massachusetts, Los Angeles, Newark, Boston, Pittsburgh
Time period: 1997-02-01--1999-01-31

The Study of Women's Health Across the Nation (SWAN) is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological, and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers and women learn how mid-life experiences affect health and quality of life during aging. The data include questions about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause.

The study is co-sponsored by the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR), the National Institutes of Health (NIH), and the NIH Office of Research on Women's Health. The study began in 1994. Between 1997 and 1999, 2,881 of the 3,302 women that joined SWAN were seen for their first follow-up visit. The research centers are located in the following communities: Detroit, MI; Boston, MA; Chicago, IL; Oakland and Los Angeles, CA; Newark, NJ; and Pittsburgh, PA. SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures.

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Survey of Holt Adoptees and Their Families, 2005 (ICPSR 4637)

Released/updated on: 2007-03-26
Geographic coverage: United States
This study, conducted January 2004 to June 2006, was undertaken to assess the health status, educational attainment, and income of adult Korean-American adoptees and their adoptive families. The study focused on families who adopted a Korean-American child through Holt International Children's Services from 1970 to 1980. The principal investigator hoped to identify the effects of large-scale changes in family environment on children's outcomes using data on adults who were adopted in infancy. Korean-American adoptees placed through Holt International Children's Services had been quasi-randomly assigned to these families in infancy using a queuing (first-come, first-served) policy. One adoptive parent from each family was surveyed, as well as a small subset of adult adoptees, and each case represented an adopted or non-adopted child in the family. Adoptive parents were asked to give their age, sex, marital status, occupation, education level, household income, height, weight, tobacco and alcohol usage, and the number of children they had. Adoptive parents also gave information on their adopted and non-adopted children's age, sex, marital status, education level, income, weight, height, undergraduate institution, number of children, and whether their children smoked, drank alcohol, or had asthma. For adopted children, parents gave the arrival age of the child and whether the child was adopted through Holt International. Adoptive parents also indicated whether they were aware of and had used services such as workshops and referral services offered by Holt. Since the survey relied on parent reports of their adult children's outcomes, surveys were also sent to a small subset of adoptees. Their surveys included the same questions asked of their adoptive parents, as well as the adoptee's value of assets, religion, and frequency of religious attendance. The study also contained information on adoptees' birth parents obtained from Holt International's administrative records and constructed variables that analyzed household composition, population characteristics, and the education and health status of the adoptive family.